ENST00000342992.11:c.87321C>A
(TTN)
|
ENSP00000343764.6:p.Ile29107=
|
|
ENST00000342175.11:c.68406C>A
(TTN)
|
ENSP00000340554.6:p.Ile22802=
|
|
ENST00000359218.10:c.68205C>A
(TTN)
|
ENSP00000352154.5:p.Ile22735=
|
|
ENST00000342175.10:c.68406C>A
(TTN)
|
ENSP00000340554.6:p.Ile22802=
|
|
ENST00000342992.10:c.87321C>A
(TTN)
|
ENSP00000343764.6:p.Ile29107=
|
|
ENST00000359218.9:c.68205C>A
(TTN)
|
ENSP00000352154.5:p.Ile22735=
|
|
ENST00000460472.6:c.67830C>A
(TTN)
|
ENSP00000434586.1:p.Ile22610=
|
|
ENST00000589042.5:c.95025C>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ile31675=
|
|
ENST00000591111.5:c.90102C>A
(TTN)
|
ENSP00000465570.1:p.Ile30034=
|
|
ENST00000615779.4:c.90102C>A
(TTN)
|
ENSP00000483597.1:p.Ile30034=
|
|
NM_001256850.1:c.90102C>A
(TTN)
|
NP_001243779.1:p.Ile30034=
|
|
NM_001267550.2:c.95025C>A
(TTN)
MANE Select
|
NP_001254479.2:p.Ile31675=
|
|
NM_003319.4:c.67830C>A
(TTN)
|
NP_003310.4:p.Ile22610=
|
|
NM_133378.4:c.87321C>A
(TTN)
|
NP_596869.4:p.Ile29107=
|
|
NM_133432.3:c.68205C>A
(TTN)
|
NP_597676.3:p.Ile22735=
|
|
NM_133437.4:c.68406C>A
(TTN)
|
NP_597681.4:p.Ile22802=
|
|
NR_038271.1:n.446+22670G>T
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+3945G>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.94122C>A
(TTN)
|
XP_011510031.1:p.Ile31374=
|
|
XM_011511730.1:c.68016C>A
(TTN)
|
XP_011510032.1:p.Ile22672=
|
|
XM_011511731.1:c.67875C>A
(TTN)
|
XP_011510033.1:p.Ile22625=
|
|
XM_017004819.1:c.93918C>A
(TTN)
|
XP_016860308.1:p.Ile31306=
|
|
XM_017004820.1:c.89316C>A
(TTN)
|
XP_016860309.1:p.Ile29772=
|
|
XM_017004821.1:c.89313C>A
(TTN)
|
XP_016860310.1:p.Ile29771=
|
|
XM_017004822.1:c.86355C>A
(TTN)
|
XP_016860311.1:p.Ile28785=
|
|
XM_017004823.1:c.67971C>A
(TTN)
|
XP_016860312.1:p.Ile22657=
|
|
XM_024453094.1:c.89466C>A
(TTN)
|
XP_024308862.1:p.Ile29822=
|
|
XM_024453095.1:c.89463C>A
(TTN)
|
XP_024308863.1:p.Ile29821=
|
|
XM_024453096.1:c.88896C>A
(TTN)
|
XP_024308864.1:p.Ile29632=
|
|
XM_024453097.1:c.86238C>A
(TTN)
|
XP_024308865.1:p.Ile28746=
|
|
XM_024453098.1:c.86157C>A
(TTN)
|
XP_024308866.1:p.Ile28719=
|
|
XM_024453099.1:c.67920C>A
(TTN)
|
XP_024308867.1:p.Ile22640=
|
|
XM_024453100.1:c.57774C>A
(TTN)
|
XP_024308868.1:p.Ile19258=
|
|